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01 1M/s Aurore Pharmaceuticals Private Limited
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01 1Camostat Mesilate JP
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01 1WC-0119
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01 1India
Date of Issue : 2022-09-19
Valid Till : 2025-07-02
Written Confirmation Number : WC-0119
Address of the Firm : Plot No. 35, 36, 38, 39,40,49, 50 & 51, Phase-IV, IDA, Jeedimetla, Medchal- Malk...
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PharmaCompass offers a list of Camostat API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Camostat manufacturer or Camostat supplier for your needs.
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PharmaCompass also assists you with knowing the Camostat API Price utilized in the formulation of products. Camostat API Price is not always fixed or binding as the Camostat Price is obtained through a variety of data sources. The Camostat Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Foipan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Foipan, including repackagers and relabelers. The FDA regulates Foipan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Foipan API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Foipan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Foipan supplier is an individual or a company that provides Foipan active pharmaceutical ingredient (API) or Foipan finished formulations upon request. The Foipan suppliers may include Foipan API manufacturers, exporters, distributors and traders.
click here to find a list of Foipan suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Foipan written confirmation (Foipan WC) is an official document issued by a regulatory agency to a Foipan manufacturer, verifying that the manufacturing facility of a Foipan active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Foipan APIs or Foipan finished pharmaceutical products to another nation, regulatory agencies frequently require a Foipan WC (written confirmation) as part of the regulatory process.
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